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Varaico: Literature-Extracted Genetic Variants
hg38
Include likely false extractions
Gene:
ROR2
Variant:
p.V787M
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ROR2
NM_004560.4:p.V787M
hg38:chr9:91724135 C>T
Frequencies & domains
Associated Papers
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome.
van Bokhoven H et al.
Nature Genetics,
2000
10932187 (PubMed
)
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